Production Operator jobs at Crown Health Care Laundry Services - 62 jobs

Versiti is a fusion of donors, scientific curiosity, and precision medicine that recognize the gifts of blood and life are precious. We are home to the world-renowned Blood Research Institute, we enable life saving gifts from our donors, and provide the science behind the medicine through our diagnostic laboratories. Versiti brings together outstanding minds with unparalleled experience in transfusion medicine, transplantation, stem cells and cellular therapies, oncology and genomics, diagnostic lab services, and medical and scientific expertise. This combination of skill and knowledge results in improved patient outcomes, higher quality services and reduced cost of care for hospitals, blood centers, hospital systems, research and educational institutions, and other health care providers. At Versiti, we are passionate about improving the lives of patients and helping our healthcare partners thrive. Position Summary Under the direction of the department leadership, prepares quality biological blood components within the prescribed time following regulatory and operational standards as specified in the Standard Operating Procedures and departmental procedures. WHEN YOU WILL WORK: Swing Shift between 1st & 2nd:Monday-Friday, anywhere between 7am-930pm (8hr shifts) On-call availbility as needed Full Time, Non-Exempt role Training schedule may differ from traditional schedule. COMPENSATION: $18.04/hr.+ based on experience - paid training provided Benefits eligible including medical/dental/vision insurance options, 7% 401(k) match, EAP, employee wellness program, generous PTO, and more. Shift differentials for evenings/weekends Evenings (after 6:00pm) - $1.50/hr. Weekends - $2.00/hr. Total Rewards Package Benefits Versiti provides a comprehensive benefits package based on your job classification. Full-time regular employes are eligible for Medical, Dental, and Vision Plans, Paid Time Off (PTO) and Holidays, Short- and Long-term disability, life insurance, 7% match dollar for dollar 401(k), voluntary programs, discount programs, others. Responsibilities Manufactures Red Blood Cells (RBCs), Fresh Frozen Plasma and Recovered Plasma Manufactures Neonatal RBCs. Sterile docks Pedipaks to Platelet Apheresis, Neonatal RBCs Performs leukoreduction of Whole Bloods and RBCs Manufactures Cryoprecipitate, Pooled Cryoprecipitate and Cryo Reduced Plasma Labels products to meet regulatory and inventory requirements Manufactures additional specialty products as needed by customer base Follows procedures pertaining to the proper storage of RBCs, platelet products and frozen products Performs and documents equipment function checks and QC as required Maintains a level of productivity that allows department to achieve production goals Works weekend, holiday rotations and on-call, as needed Other duties, as assigned Performs other duties as assigned Complies with all policies and standards Qualifications Education High School Diploma required equivalent required Experience Less than 1 year 1-6 months related experience and/or training or equivalent combination of education and experience required Knowledge, Skills and Abilities Ability to read, interpret, and write documents such as operating forms, operating and maintenance instructions, and other department manuals required Above average attention to detail and problem-solving skills required Ability to apply judgment to written or oral instructions required Aptitude for computers and data entry skills required Ability to manage interruptions in a fast-paced environment required Customer service and communication skills required Able to organize work to provide productive work flow needed in component manufacturing required Flexibility to work independently and with a team required Organized, able to prioritize and handle multiple tasks at one time required Be able and available to work a flexible working schedule as required based on volume and timing of blood collections required Ability to work independently with limited written or oral instruction required Understands military time required Tools and Technology General office equipment (computer, printer, fax, copy machine) required Microsoft Suite (Word, Excel, PowerPoint, Outlook) required Software systems (Blood Establishment Computer Systems, Title21) required Lab specific equipment, including, but not limited to: • Sealers • Centrifuge • Water bath • Scales required

reports to a Supervisor, Manufacturing. This entry-level position involves working with a small team in a GMP environment to manufacture commercial and/or clinical-scale batches. Essential Functions: The essential functions of this position include: Production, bulk packaging, and inspection of pharmaceutical drug formulations Assisting with facility cleaning and operational maintenance Cleaning all manufacturing equipment and areas Assisting with facility and process validations as required Assisting with environmental and water system monitoring as required Assisting with RCRA and safety inspections as required Documenting all work as required by cGMPs and GDPs on a timely basis Reading and following all Company SOPs and guidelines Abiding by all safety requirements as defined by the company Completing other tasks as assigned by supervision Preferred Qualifications: Basic knowledge of the Scientific Method Basic math skills including addition, subtraction, multiplication, division, and percentages Basic knowledge of and adherence to current GMPs and GDPs Basic knowledge of chemistry and biology Basic knowledge of HAZCOM, RCRA, and other Safety requirements Basic level of mechanical aptitude Good documentation skills Ability to learn how to operate all types of production equipment (i.e. Blenders, HMIs, Tablet presses, Coaters, Wash off lines, Comils, etc.) Ability to read, understand, and accurately follow company SOPs and guidelines Basic knowledge of computer systems (Microsoft Suite, SAP, Veeva Vault, LMS) Understanding and comprehension of Master Batch Records Detail-oriented Willingness to learn new tasks and skills Ability to work well in a team environment Ability to respond quickly and execute assignments Willingness to readily adapt to changing job duties Positive attitude Understanding of and promotion of company and customer objectives Ability to follow all procedures to ensure a high-quality product Education and Experience: Manufacturing Associate I Basic Qualifications: High School diploma or equivalent Preferred Qualifications: 0-1 years of experience in a pharmaceutical manufacturing operation, preferably in OSD A bachelor's degree is preferred; other relevant work experience, education, and training will be considered. Manufacturing Associate II Basic Qualifications High School diploma or equivalent 1-3 years of experience in a pharmaceutical manufacturing operation. Preferred Qualifications 1+ year experience in OSD Manufacturing Associate degree or higher in a science/technical discipline Other relative work experience, education, and training will be considered Manufacturing Associate III Basic Qualifications High School diploma or equivalent 4-5 years of experience in a pharmaceutical manufacturing operation. Preferred Qualifications 2-3 year experience in OSD Manufacturing Associate degree or higher in a science/technical discipline Other relative work experience, education, and training will be considered Working Conditions: Available for any shift with the possibility for overtime (as necessary) Physical Requirements: Ability to push and/or pull equipment or product using a pallet jack Ability to lift/move 40 lbs. overhead. Ability to properly gown and don PAPR for potent controlled substance formulations for extended periods of time Must be able to be medically cleared for respirator use (PAPR) Ability to operate different types of production equipment. Ability to gown correctly for clean room manufacturing operations. Ability to stand or sit for extended periods (up to 4 hours at a time). Must be able to work in an office and a manufacturing environment.

is based in Wilmington, OH We are seeking a qualified candidate for this position, which is available on both the 1st and 2nd shifts. While we will consider applicants for either shift, preference will be given to those available for 2nd shift. Summary: Perform all necessary operation activities related to filling of microsphere/suspension/liquid products. These activities include but are not limited to the following: Equipment Cleaning/Assembly/Setup, Equipment Operation, Batch processing. Read and follow detailed written SOP/MPR's with thorough documentation of operations according to cGMP. Ability to aseptically gown and maintain gowning qualification. Perform Area Sanitizations as needed. Maintain individual training proficiency through individual Learning Management System. Job Description: * Read and follow detailed written SOP's/MPR's/Procedures. * Document all work as required by cGMP's on a timely basis. * Execute tasks as directed with close attention to detail. * Monitors process with close attention to detail. * Follows Alkermes internal policies. * Abide by all safety requirements as defined by the company. * Perform Aseptic Gowning and maintaining gowning qualification. (this includes wearing of hood, coverall, boots, mask, goggles, gloves) * Perform clean room sanitizations. * Perform equipment prep/assembly/setup. * Operate equipment used in filling of microspheres/suspensions/liquid products. * Assist with Development and Validation activities as required. * Other tasks as assigned by Manager. * Shift coverage and weekend work may be required. SKILLS/ABILITIES: * General knowledge of aseptic fundamentals. * General math skills, including using metric weight system. * General Knowledge and Adherence to Current Good Manufacturing Practices. * General Knowledge HAZCOM RCRA, and other safety requirements. * Good level of mechanical aptitude; ability to perform minor non-routine equipment adjustments and diagnose improperly operating equipment. * General computer skills. * Excellent documentation skills. PERSONAL ATTRIBUTES: * Positive Attitude * Integrity/Ethics * Adaptability/Flexibility * Dependability * Detailed Oriented * Self-Motivated * Responds Quickly to Assignments * Works Well in a Team Environment. * Adapts Well to Changing job duties. * Takes Ownership and is Willing to Learn new tasks/skills Physical Requirements: * Occasional periods of repetitive motion. * Aseptic gowning must be maintained, including an annual requalification. * Walking, lifting, pushing and pulling carts, reaching, climbing, and bending may all be required. * Ability to operate all types of production equipment (i.e., Rockwell HMI, Autoclaves, etc.) * Ability to read, understand, and accurately follow company SOP's and guidelines. * Ability to lift/move up to 50 lbs. overhead. Ability to team lift up to 100 lbs. * Ability to stand in steel-toed shoes for a minimum of 7 hrs. Minimum Education & Experience Requirements: MANUFACTURING ASSOCIATE 1 Basic Requirements: * High School diploma or equivalent. Preferred Requirements: * 0-1 year of experience in a sterile pharmaceutical operation. * Associates degree or higher in science/technical discipline. MANUFACTURING ASSOCIATE 2 Basic Qualifications: * High School diploma or equivalent. * 1-3 years of pharmaceutical manufacturing or equivalent experience. Preferred Qualifications: * 1+ year in a sterile pharmaceutical operation. * Associates degree or higher in science/technical discipline. MANUFACTURING ASSOCIATE 3 Basic Qualifications: * High school diploma or equivalent. * 4-5 years of pharmaceutical manufacturing or equivalent experience. Preferred Qualifications: * 2-3 years of experience in a sterile pharmaceutical operation. * Associates degree or higher in science/technical discipline #LI-AH1

Job Description The Machine Operator will be responsible for the operation of manufacturing machinery utilized in a high-quality medical device manufacturing environment. Shift Hours: 7:00 PM - 5:30 AM Monday - Thursday What You'll do as a Machin Operator Set-up and operate assembly equipment using prescribed methods and training to manufacture parts within acceptable tolerances and standards. Replace raw materials as required during the setup process and during continuous runs of production lots. Continuous monitoring of assemble equipment while making in-process adjustments to ensure product conforms to specification. Use required measuring instruments and gages or scales to check and ensure products meet specifications Perform prescribed cleaning of equipment Perform routine general maintenance when scheduled Compliance with STERIS Quality System policies and procedures pertaining to manufacturing processes. Communicate clearly with personnel and assigned work group. Perform work to meet all required quality specifications. Maintain and follow all safety standards. Other duties as assigned. The Experience, Skills and Abilities Needed **Required: ** High School Diploma or GED. 3 years of Manufacturing Experience. **Preferred: ** Minimum of 3 years of experience working with machinery in a manufacturing environment. **Other: ** Must be able to use measuring instruments, gages, and scales. Must demonstrate ability to manufacture products according to the procedures and drawings while maintaining quality systems and standards. Must be mechanically inclined and be able to think quickly in order to make in-process adjustments in a timely manner. Must have good communication skills. Must be able to work in a team environment. Must have ability to stand for long periods of time. Must be capable of lifting 50 pounds without assistance. What STERIS Offers We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being, and financial future. *Here is just a brief overview of what we offer: * Market Competitive Pay Extensive Paid Time Off and (9) added holidays Excellent Healthcare, Dental and Vision Benefits Long/Short Term disability coverage 401(k) with company match Maternity & Paternal Leave Additional add-on benefits/discounts for programs such as Pet Insurance Tuition Reimbursement and continued educations programs Excellent opportunities for advancement and stable long-term career

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. The Machine Operator will be responsible for the operation of manufacturing machinery utilized in a high-quality medical device manufacturing environment. Shift Hours: 7:00 PM - 5:30 AM Monday - Thursday What You'll do as a Machine Operator * Set-up and operate assembly equipment using prescribed methods and training to manufacture parts within acceptable tolerances and standards. * Replace raw materials as required during the setup process and during continuous runs of production lots. * Continuous monitoring of assemble equipment while making in-process adjustments to ensure product conforms to specification. * Use required measuring instruments and gages or scales to check and ensure products meet specifications * Perform prescribed cleaning of equipment * Perform routine general maintenance when scheduled * Compliance with STERIS Quality System policies and procedures pertaining to manufacturing processes. * Communicate clearly with personnel and assigned work group. * Perform work to meet all required quality specifications. * Maintain and follow all safety standards. * Other duties as assigned. The Experience, Skills and Abilities Needed Required: * High School Diploma or GED. * 3 years of Manufacturing Experience. Preferred: * Minimum of 3 years of experience working with machinery in a manufacturing environment. Other: * Must be able to use measuring instruments, gages, and scales. * Must demonstrate ability to manufacture products according to the procedures and drawings while maintaining quality systems and standards. * Must be mechanically inclined and be able to think quickly in order to make in-process adjustments in a timely manner. * Must have good communication skills. * Must be able to work in a team environment. * Must have ability to stand for long periods of time. * Must be capable of lifting 50 pounds without assistance. What STERIS Offers We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being, and financial future. Here is just a brief overview of what we offer: * Market Competitive Pay * Extensive Paid Time Off and (9) added holidays * Excellent Healthcare, Dental and Vision Benefits * Long/Short Term disability coverage * 401(k) with company match * Maternity & Paternal Leave * Additional add-on benefits/discounts for programs such as Pet Insurance * Tuition Reimbursement and continued educations programs * Excellent opportunities for advancement and stable long-term career Pay rate for this opportunity is $20.24. This position is eligible for bonus participation. Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc. STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits Open until position is filled. STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. The Machine Operator will be responsible for the operation of manufacturing machinery utilized in a high-quality medical device manufacturing environment. Shift Hours: 7:00 PM - 5:30 AM Monday - Thursday What You'll do as a Machine Operator Set-up and operate assembly equipment using prescribed methods and training to manufacture parts within acceptable tolerances and standards. Replace raw materials as required during the setup process and during continuous runs of production lots. Continuous monitoring of assemble equipment while making in-process adjustments to ensure product conforms to specification. Use required measuring instruments and gages or scales to check and ensure products meet specifications Perform prescribed cleaning of equipment Perform routine general maintenance when scheduled Compliance with STERIS Quality System policies and procedures pertaining to manufacturing processes. Communicate clearly with personnel and assigned work group. Perform work to meet all required quality specifications. Maintain and follow all safety standards. Other duties as assigned. The Experience, Skills and Abilities Needed Required: High School Diploma or GED. 3 years of Manufacturing Experience. Preferred: Minimum of 3 years of experience working with machinery in a manufacturing environment. Other: Must be able to use measuring instruments, gages, and scales. Must demonstrate ability to manufacture products according to the procedures and drawings while maintaining quality systems and standards. Must be mechanically inclined and be able to think quickly in order to make in-process adjustments in a timely manner. Must have good communication skills. Must be able to work in a team environment. Must have ability to stand for long periods of time. Must be capable of lifting 50 pounds without assistance. What STERIS Offers We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being, and financial future. Here is just a brief overview of what we offer: Market Competitive Pay Extensive Paid Time Off and (9) added holidays Excellent Healthcare, Dental and Vision Benefits Long/Short Term disability coverage 401(k) with company match Maternity & Paternal Leave Additional add-on benefits/discounts for programs such as Pet Insurance Tuition Reimbursement and continued educations programs Excellent opportunities for advancement and stable long-term career Pay rate for this opportunity is $20.24. This position is eligible for bonus participation. Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc. STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits Open until position is filled. STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.

About Abeona Our Values: Patient First | Innovation | Integrity | Determination | Trust Join us in making cure the new standard of care. At Abeona Therapeutics, we exist for our patients and their caregivers; their needs guide our decision-making. We challenge ourselves to think differently, move quickly, and deliver solutions. We hold ourselves to the highest ethical and quality standards. We persevere with resilience and focus to achieve our mission. We build trust through humility, mutual appreciation, openness, and respect. Company Description Abeona Therapeutics Inc. is a commercial-stage biopharmaceutical company focused on developing cell and gene therapies for serious diseases. Notably, Abeona's ZEVASKYN™ (prademagene zamikeracel) is the first autologous cell-based gene therapy treating wounds in adults and pediatric patients with recessive dystrophic epidermolysis bullosa (RDEB). The company's cGMP manufacturing facility in Cleveland, Ohio, is dedicated to producing ZEVASKYN™. Abeona's portfolio includes adeno-associated virus (AAV)-based gene therapies for ophthalmic diseases with unmet medical needs, and their novel AAV capsids aim to improve treatment outcomes for various debilitating conditions. Position Overview Abeona is looking for a Manufacturing Associate to join our team in Cleveland, OH. The successful candidate will be responsible for Manufacturing initiatives supporting multiple product pipelines. The candidate will be an integral part of a fast-paced group responsible for the manufacture of retroviral vector, autologous gene-corrected cell therapies, and clinical AAV gene therapies. Responsibilities will include executing protocols and manufacturing clinical material across multiple products as well as supporting process optimization work and document generation. The ideal candidate will have experience in production of biologics in a controlled cGXP setting. Strong aseptic and cell culture technique as well as collaborative work in a team is an integral part of this position. Schedule: The current manufacturing team schedule is Monday to Friday, with occasional weekend shifts. The manufacturing team will be transitioning into a 4-day work week with 10-hour shifts in the near future. These days will be Sunday - Wednesday and Wednesday to Sunday. Essential Duties and Responsibilities Produce cell therapies in cGMP facility in conjunction with manufacturing production records (MPRs). Execute studies in support of process optimization and validation. Author, review, and provide technical support for manufacturing SOPs and MPRs. Identify, suggest, and manage projects in parallel with manufacturing activities to reach set goals. Ability to collaborate with others while maintaining a strong capability in independent, critical thought. Strong organizational skills required. Must be able to work as part of a team. Contribute to activities that support safety and/or lab infrastructure. Qualifications BS or equivalent in scientific discipline and min of 2-4 years related lab experience or MS or equivalent with 1-2 years of experience. General biological lab experience. Experience with mammalian and/or insect cell culture technology. Familiarity with aseptic technique, cell culture, and cell counters is strongly preferred. Previous GXP experience. Experience with production processes for cell therapies and/or viral vectors or vaccines is highly preferred. A strong background in the fundamentals and scale-up of production of biologic molecules strongly preferred. Additional Desired Skills and Abilities: Advanced communication and organizational skills. Advanced interpersonal skills and the ability to work with individuals across all organizational levels. Attention to detail and accuracy. Detailed record keeping and data documentation. Demonstrated project management skills. Ability to read, analyze, and interpret technical procedures, publications, intellectual property and/or government documents. Working knowledge of GLP, GDP, GCP and GMP regulations and their ISO counterparts and ICH Guidelines. High level of proficiency with Microsoft Office programs. Less than 10% travel. Any travel will be reimbursed in accordance with company policy Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to experience prolonged sitting, some bending, stooping and stretching. Hand-eye coordination and manual dexterity sufficient to operate office equipment is required. A normal range of hearing and vision correctable to 20/20 is required. Occasional lifting of up to 50 pounds is required. Benefits Our values apply to how we view caring for each other as well. While the patient comes first, our employees are vital to making that happen, and so we strive to offer a competitive benefits package that includes: Medical insurance coverage (multiple options to meet our employees' and their families' needs) Dental and vision coverage 401k match plan Lifestyle spending account Compensation (annual): $70,000 - $$73,700 (please note that this range includes annual salary and the maximum anticipated annual bonus) Visa Sponsorship Not Currently Available IMPORTANT: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Job Description About Abeona Our Values: Patient First | Innovation | Integrity | Determination | Trust Join us in making cure the new standard of care. At Abeona Therapeutics, we exist for our patients and their caregivers; their needs guide our decision-making. We challenge ourselves to think differently, move quickly, and deliver solutions. We hold ourselves to the highest ethical and quality standards. We persevere with resilience and focus to achieve our mission. We build trust through humility, mutual appreciation, openness, and respect. Company Description Abeona Therapeutics Inc. is a commercial-stage biopharmaceutical company focused on developing cell and gene therapies for serious diseases. Notably, Abeona's ZEVASKYN™ (prademagene zamikeracel) is the first autologous cell-based gene therapy treating wounds in adults and pediatric patients with recessive dystrophic epidermolysis bullosa (RDEB). The company's cGMP manufacturing facility in Cleveland, Ohio, is dedicated to producing ZEVASKYN™. Abeona's portfolio includes adeno-associated virus (AAV)-based gene therapies for ophthalmic diseases with unmet medical needs, and their novel AAV capsids aim to improve treatment outcomes for various debilitating conditions. Position Overview Abeona is looking for a Manufacturing Associate to join our team in Cleveland, OH. The successful candidate will be responsible for Manufacturing initiatives supporting multiple product pipelines. The candidate will be an integral part of a fast-paced group responsible for the manufacture of retroviral vector, autologous gene-corrected cell therapies, and clinical AAV gene therapies. Responsibilities will include executing protocols and manufacturing clinical material across multiple products as well as supporting process optimization work and document generation. The ideal candidate will have experience in production of biologics in a controlled cGXP setting. Strong aseptic and cell culture technique as well as collaborative work in a team is an integral part of this position. Schedule: The current manufacturing team schedule is Monday to Friday, with occasional weekend shifts. The manufacturing team will be transitioning into a 4-day work week with 10-hour shifts in the near future. These days will be Sunday - Wednesday and Wednesday to Sunday. Essential Duties and Responsibilities Produce cell therapies in cGMP facility in conjunction with manufacturing production records (MPRs). Execute studies in support of process optimization and validation. Author, review, and provide technical support for manufacturing SOPs and MPRs. Identify, suggest, and manage projects in parallel with manufacturing activities to reach set goals. Ability to collaborate with others while maintaining a strong capability in independent, critical thought. Strong organizational skills required. Must be able to work as part of a team. Contribute to activities that support safety and/or lab infrastructure. Qualifications BS or equivalent in scientific discipline and min of 2-4 years related lab experience or MS or equivalent with 1-2 years of experience. General biological lab experience. Experience with mammalian and/or insect cell culture technology. Familiarity with aseptic technique, cell culture, and cell counters is strongly preferred. Previous GXP experience. Experience with production processes for cell therapies and/or viral vectors or vaccines is highly preferred. A strong background in the fundamentals and scale-up of production of biologic molecules strongly preferred. Additional Desired Skills and Abilities: Advanced communication and organizational skills. Advanced interpersonal skills and the ability to work with individuals across all organizational levels. Attention to detail and accuracy. Detailed record keeping and data documentation. Demonstrated project management skills. Ability to read, analyze, and interpret technical procedures, publications, intellectual property and/or government documents. Working knowledge of GLP, GDP, GCP and GMP regulations and their ISO counterparts and ICH Guidelines. High level of proficiency with Microsoft Office programs. Less than 10% travel. Any travel will be reimbursed in accordance with company policy Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to experience prolonged sitting, some bending, stooping and stretching. Hand-eye coordination and manual dexterity sufficient to operate office equipment is required. A normal range of hearing and vision correctable to 20/20 is required. Occasional lifting of up to 50 pounds is required. Benefits Our values apply to how we view caring for each other as well. While the patient comes first, our employees are vital to making that happen, and so we strive to offer a competitive benefits package that includes: Medical insurance coverage (multiple options to meet our employees' and their families' needs) Dental and vision coverage 401k match plan Lifestyle spending account Compensation (annual): $70,000 - $$73,700 (please note that this range includes annual salary and the maximum anticipated annual bonus) Visa Sponsorship Not Currently Available IMPORTANT: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

About Abeona Our Values: Patient First | Innovation | Integrity | Determination | Trust Join us in making cure the new standard of care. At Abeona Therapeutics, we exist for our patients and their caregivers; their needs guide our decision-making. We challenge ourselves to think differently, move quickly, and deliver solutions. We hold ourselves to the highest ethical and quality standards. We persevere with resilience and focus to achieve our mission. We build trust through humility, mutual appreciation, openness, and respect. Company Description Abeona Therapeutics Inc. is a commercial-stage biopharmaceutical company focused on developing cell and gene therapies for serious diseases. Notably, Abeona's ZEVASKYN (prademagene zamikeracel) is the first autologous cell-based gene therapy treating wounds in adults and pediatric patients with recessive dystrophic epidermolysis bullosa (RDEB). The company's cGMP manufacturing facility in Cleveland, Ohio, is dedicated to producing ZEVASKYN. Abeona's portfolio includes adeno-associated virus (AAV)-based gene therapies for ophthalmic diseases with unmet medical needs, and their novel AAV capsids aim to improve treatment outcomes for various debilitating conditions. Position Overview Abeona is looking for a Manufacturing Associate to join our team in Cleveland, OH. The successful candidate will be responsible for Manufacturing initiatives supporting multiple product pipelines. The candidate will be an integral part of a fast-paced group responsible for the manufacture of retroviral vector, autologous gene-corrected cell therapies, and clinical AAV gene therapies. Responsibilities will include executing protocols and manufacturing clinical material across multiple products as well as supporting process optimization work and document generation. The ideal candidate will have experience in production of biologics in a controlled cGXP setting. Strong aseptic and cell culture technique as well as collaborative work in a team is an integral part of this position. Schedule: The current manufacturing team schedule is Monday to Friday, with occasional weekend shifts. The manufacturing team will be transitioning into a 4-day work week with 10-hour shifts in the near future. These days will be Sunday - Wednesday and Wednesday to Sunday. Essential Duties and Responsibilities * Produce cell therapies in cGMP facility in conjunction with manufacturing production records (MPRs). * Execute studies in support of process optimization and validation. * Author, review, and provide technical support for manufacturing SOPs and MPRs. * Identify, suggest, and manage projects in parallel with manufacturing activities to reach set goals. * Ability to collaborate with others while maintaining a strong capability in independent, critical thought. * Strong organizational skills required. * Must be able to work as part of a team. * Contribute to activities that support safety and/or lab infrastructure. Qualifications * BS or equivalent in scientific discipline and min of 2-4 years related lab experience or MS or equivalent with 1-2 years of experience. * General biological lab experience. * Experience with mammalian and/or insect cell culture technology. * Familiarity with aseptic technique, cell culture, and cell counters is strongly preferred. * Previous GXP experience. * Experience with production processes for cell therapies and/or viral vectors or vaccines is highly preferred. * A strong background in the fundamentals and scale-up of production of biologic molecules strongly preferred. Additional Desired Skills and Abilities: * Advanced communication and organizational skills. * Advanced interpersonal skills and the ability to work with individuals across all organizational levels. * Attention to detail and accuracy. * Detailed record keeping and data documentation. * Demonstrated project management skills. * Ability to read, analyze, and interpret technical procedures, publications, intellectual property and/or government documents. * Working knowledge of GLP, GDP, GCP and GMP regulations and their ISO counterparts and ICH Guidelines. * High level of proficiency with Microsoft Office programs. * Less than 10% travel. Any travel will be reimbursed in accordance with company policy Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to experience prolonged sitting, some bending, stooping and stretching. Hand-eye coordination and manual dexterity sufficient to operate office equipment is required. A normal range of hearing and vision correctable to 20/20 is required. Occasional lifting of up to 50 pounds is required. Benefits Our values apply to how we view caring for each other as well. While the patient comes first, our employees are vital to making that happen, and so we strive to offer a competitive benefits package that includes: * Medical insurance coverage (multiple options to meet our employees' and their families' needs) * Dental and vision coverage * 401k match plan * Lifestyle spending account * Compensation (annual): $70,000 - $$73,700 (please note that this range includes annual salary and the maximum anticipated annual bonus) Visa Sponsorship Not Currently Available IMPORTANT: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

The Production Technician is responsible for all aspects of plant processing from post-crop harvest through packaging and labeling of the final product ready for customer sale as outlined by the management team and SOPs. These responsibilities include post-harvest tasks including the drying and curing stage all the way through trimming, packaging, and labeling the product. This position works in a timely manner and strives to increase productivity and acts with professional regard to the management and use of all production facilities and processing equipment. Major Areas of Responsibility include: * Assists in the post-harvest plant processing of cannabis. * Fan leaf removal, harvest, drying, trimming, curing, weighing, packaging, labeling, recording, and inspection of product in addition to cleaning and sanitation. * Maintains a clean and organized work environment. * Transport harvested plants to drying room and hang to be dried. * Hand trims and/or operates a trimming machine to remove excess plant material. * Weighs, records, and shreds plants waste and adds a non-cannabis medium for compliant disposal. * Receives instructions and assists on tasks as delegated by management team. * Works in a quick and efficient manner. * Complies with all HR policies including confidentiality and non-disclosure. Minimum Qualifications (Skills, Knowledge & Abilities): * All applicants must be at least 21 years of age. * 1-3 years of experience in production position; including hands-on production activities. * General knowledge of weights and measurement. * Evening/night/weekend work may be required. * Speed and precision with equipment and attention to detail. * Ability to multi-task and maintain work consistency on a daily basis. * High attention to detail. * Standing/sitting for long periods of time. Travel %: 0 FLSA status: Non-exempt Additional Abilities Required: * Exposure to pollen, dust, and plant particles due to the handling of raw plant materials. * The job requires physical activity, including prolonged sitting, standing, repetitive bending, climbing, and lifting or moving up to 50 pounds (or more with a coworker). Good visual acuity, hand-eye coordination, manual dexterity, and ability to perform repetitive motions with accuracy is required. The noise level in the work environment is usually moderate. Note: Nothing in this job description restricts the company's right to assign or reassign duties and responsibilities to this position at any time. Reasonable accommodations may be made in appropriate circumstances to enable individuals to perform the essential functions of the position. About The Cannabist Company (f/k/a Columbia Care) The Cannabist Company, formerly known as Columbia Care, is one of the most experienced cultivators, manufacturers and providers of cannabis products and related services, with licenses in 14 U.S. jurisdictions. The Company operates 89 facilities including 70 dispensaries and 19 cultivation and manufacturing facilities, including those under development. Columbia Care, now The Cannabist Company, is one of the original multi-state providers of cannabis in the U.S. and now delivers industry-leading products and services to both the medical and adult-use markets. In 2021, the Company launched Cannabist, its retail brand, creating a national dispensary network that leverages proprietary technology platforms. The company offers products spanning flower, edibles, oils and tablets, and manufactures popular brands including dreamt, Seed & Strain, Triple Seven, Hedy, gLeaf, Classix, Press, and Amber. For more information, please visit ************************

Element has an opportunity for a Machine Operator (3rd Shift) to join our rapidly expanding team. As a member of the operations team, the Machining position performs a variety of routine and non-routine machining assignments within the department assigned and insures timely and accurate test results under direct supervision. The operator position must be proficient in a number of core business skills including but not limited to compliance to established safety rules, code of conduct, and company policies and procedures. Salary: $25- $30/hr DOE Responsibilities * Using cutting equipment to prepare specimens for testing as dictated in customer specifications * Maintain equipment and schedules preventative maintenance * Frequently provided guidance from Department Manager, Machinist/Senior Machinist coworkers * Gathering and recording dimensions in accordance with quality assurance requirements Skills / Qualifications * Working knowledge of laboratory safety * HS diploma or GED certificate preferred. College or vocational school coursework welcomed * Some college level courses completed and/or a minimum of 2 years' experience in a machine shop environment * Understanding of machining concepts * Preferred - have earned Associate degree mechanical related field * Basic understanding of machining concepts, measuring instruments and dimensional concepts * Working knowledge of machine shop safety protocol * Strong computer skills * Ability to apply concepts of basic algebra and geometry a plus Physical Demands: * Frequency of required physical force: Moderate. * Lifting requirements: lifting 50 lbs. on occasion. * Ability to stand on feet for long periods of time. * Ability to lift 50+lbs periodically. #LI-TK1 Company Overview Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to 'Make tomorrow safer than today'. When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access. While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development. Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization. Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming "the world's most trusted testing partner". All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws.

Line Crew, 2nd Shift JOIN A TEAM THAT CHANGES LIVES Principle Business Enterprises, Inc. (PBE) is a family-run, value-driven organization with big hearts and true passion for what we do. Celebrating over 60 years of service to the healthcare field and over 30 years as a pioneer in the development of incontinence and moisture management solutions, we're living our mission to improve the lives of caregivers, those who wear our products and our workforce. Our commitment includes innovative and life-changing products; positive partnerships with customers and suppliers; wellbeing programs that support our Associates and their families; and community support. We offer excellent health benefits including free access to onsite and a local health clinic, paid personal and vacation time, an annual profit-sharing bonus, a 401k plan with a company match, company-paid disability and life insurance, and more. We also offer many perks that recognize our associates' hard work and allow them to have fun! We are a safe and clean manufacturing plant looking for respectful, team-oriented candidates who have a great work ethic and thrive in a fast-paced environment focused on safety, continuous improvement and producing quality products that help the lives of others. Learn more about PBE's culture and benefits by clicking here. Bag and package absorbent products efficiently so as to maintain constant flow of production. Starting pay is $18.50. SPECIFIC RESPONSIBILITIES: Pull absorbent products from machine, bag, and place on bag-sealing machine Pack sealed bags of absorbent products into boxes and push through case sealer Move cases from conveyor to pallet Inspect materials, products, and containers at each step of process Sort seconds and package Label and assemble boxes Clean and complete record keeping as needed Assist on change overs as directed Read and interpret documents (safety rules, operating/maintenance instructions & procedure manuals) Fill out routine reports and communicate effectively Compute rate, ratio, and percent and draw and interpret bar graphs Utilize common sense to understand and carry out detailed but non-complex written and/or oral instructions Use basic mathematical skills (add, subtract, multiply, divide, units of measurement, whole numbers, common fractions, & decimals) MINIMUM QUALIFICATIONS: High school diploma or general education degree (GED); or three months related experience and/or training; or equivalent combination of education and experience. Previous experience in a manufacturing environment preferred Communication: must have the ability to convey and understand key job concepts in English PHYSICAL REQUIREMENTS: Must be able to stand for long periods of time; use hands to handle objects, tools, or controls; reach with hands and arms; stoop, kneel, and/or crouch. Must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds, and occasionally lift and/or move up to 50 pounds. Must have close, distance, color, & peripheral vision abilities along with depth perception and the ability to adjust focus. *Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. We are an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.

Production Associate, 3rd Shift Bowling Green NORTH JOIN A TEAM THAT CHANGES LIVES Principle Business Enterprises, Inc. (PBE) is a family-run, value-driven organization with big hearts and true passion for what we do. Celebrating over 60 years of service to the healthcare field and over 30 years as a pioneer in the development of incontinence and moisture management solutions, we're living our mission to improve the lives of caregivers, those who wear our products and our workforce. Our commitment includes innovative and life-changing products; positive partnerships with customers and suppliers; wellbeing programs that support our Associates and their families; and community support. We offer excellent health benefits including free access to onsite and a local health clinic, paid personal and vacation time, an annual profit-sharing bonus, a 401k plan with a company match, company-paid disability and life insurance, and more. We also offer many perks that recognize our associates' hard work and allow them to have fun! We are a safe and clean manufacturing plant looking for respectful, team-oriented candidates who have a great work ethic and thrive in a fast-paced environment focused on safety, continuous improvement and producing quality products that help the lives of others. Learn more about PBE's culture and benefits by clicking here. Bag and package absorbent products efficiently so as to maintain constant flow of production. This position is hourly. The base pay is $18.50 per hour. We also pay a $1.00 shift premium for 2 nd or 3 rd shift. Associates are eligible for their first pay increase after 90 days. SPECIFIC RESPONSIBILITIES: Pull absorbent products from machine, bag, and place on bag-sealing machine Pack sealed bags of absorbent products into boxes and push through case sealer Move cases from conveyor to pallet Inspect materials, products, and containers at each step of process Sort seconds and package Label and assemble boxes Clean and complete record keeping as needed Assist on change overs as directed Read and interpret documents (safety rules, operating/maintenance instructions & procedure manuals) Fill out routine reports and communicate effectively Compute rate, ratio, and percent and draw and interpret bar graphs Utilize common sense to understand and carry out detailed but non-complex written and/or oral instructions Use basic mathematical skills (add, subtract, multiply, divide, units of measurement, whole numbers, common fractions, & decimals) MINIMUM QUALIFICATIONS: High school diploma or general education degree (GED); or three months related experience and/or training; or equivalent combination of education and experience. Previous experience in a manufacturing environment preferred. Communication: must have the ability to convey and understand key job concepts in English. PHYSICAL REQUIREMENTS: Must be able to stand for long periods of time; use hands to handle objects, tools, or controls; reach with hands and arms; stoop, kneel, and/or crouch. Must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds, and occasionally lift and/or move up to 50 pounds. Must have close, distance, color, & peripheral vision abilities along with depth perception and the ability to adjust focus. *Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. We are an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.

Salary Range: $16-$18/hour As a Machine Operator in a tape manufacturing environment, you will be responsible for setting up, operating, and maintaining slitting machines to produce high-quality adhesive and tape products. This role requires precision in machine calibration, attention to detail in product inspection, and adherence to safety protocols to ensure efficient production and product compliance with specifications. Job Duties: Set up and calibrate slitting machines according to production specifications, ensuring accurate alignment and settings for different adhesive and tape materials. Operate slitting machines efficiently, monitoring for any irregularities or malfunctions. Adjust machine settings as needed to maintain product quality and production speed. Inspect finished products for defects, ensuring adherence to quality standards. Measure dimensions and assess the physical properties of slit materials to confirm compliance with specifications. Load raw materials onto the slitting machine and unload finished rolls. Properly handle and store materials to prevent damage and ensure traceability throughout the production process. Perform routine maintenance on slitting machines, including cleaning, lubrication, and minor repairs. Troubleshoot mechanical issues to minimize downtime and ensure continuous operation. Maintain accurate records of production output, machine settings, and any incidents or deviations from standard procedures. Log all maintenance activities and report any issues to supervisors. Follow all safety protocols and procedures to maintain a safe working environment. Use personal protective equipment (PPE) as required and participate in safety training programs. Work closely with the production team, quality control, and maintenance staff to ensure smooth operation and address any production challenges. Communicate effectively to coordinate efforts and achieve production goals. All other duties as assigned. Physical Requirements: Ability to lift and carry heavy materials, typically up to 50 pounds, regularly. Prolonged periods of standing and walking throughout the workday. Frequent bending, stooping, and reaching to handle materials, load machines, and pack products. Good hand-eye coordination and manual dexterity to handle small parts, operate machinery, and perform tasks requiring precision. Ability to push and pull carts, pallet jacks, or other equipment loaded with materials. Performing repetitive tasks such as packing, labeling, and operating machines. Occasionally climbing ladders or steps to access materials or equipment. Good vision, with or without corrective lenses, to inspect products for quality and read labels or instructions. Adequate hearing ability to communicate with team members and hear alarms or safety signals. Ability to maintain a steady work pace over long shifts, often in a fast-paced environment. Adherex Group is an Equal Opportunity Employer Benefits: 401(k), PTO, Holiday pay, Medical, Dental, Vision, EAP Qualifications Education and Experience: High School Diploma, GED or Equivalent Prior experience working with machines is preferred or previous experience working as a General Laborer in the manufacturing plant. Required Skills/Abilities: Ability to follow instructions and work as part of a team. Basic mechanical aptitude and the ability to operate machinery or equipment. Attention to detail and the ability to perform repetitive tasks with accuracy. Physical fitness, as the job may involve standing for extended periods and lifting or moving heavy objects. Understanding and adherence to safety protocols and procedures.

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Please take this virtual tour to get a sneak peek of one of our Plasma Donation Centers. Are you looking for a meaningful career where you can truly make an impact? Join our team, where you'll work alongside dedicated professionals who share your commitment to helping others. At BioLife, you'll find more than just a job - you'll discover a supportive, inclusive, and mission-driven culture where your contributions matter. Whether you're beginning your career or seeking new opportunities for growth, we provide clear pathways for professional development, including advancement into leadership roles. We are seeking candidates interested in establishing a long-term career within our organization and who are available to work a flexible schedule, including evenings and rotating weekends. What We Offer: * Comprehensive benefits starting on Day 1 - because your well-being matters * On-demand pay - access a portion of your earned wages before payday * Debt-free education opportunities - earn your degree or certifications with no out-of-pocket costs * Paid training - we'll set you up for success from day one * Career growth and advancement opportunities - build your future here! About the role: Every day, the donors you meet will motivate you. The high-quality plasma you collect will become life-changing medicines. Here, a commitment to customer service and quality is expected. You will report to the Plasma Center Manager and will perform as a plasma donor screener and perform phlebotomy to support plasma center operations. How you will contribute: * You will answer phones, and greet and focus on our donors, while ensuring the safety of donors and our team. * You will screen new and repeat donors and take and record donor vital signs and finger stick results. * You will use our Donor Information System, prepare donor charts, maintain accurate records, and coordinate donor compensation. * You will help identify operational opportunities for continuous improvement and initiate changes to center processes using company approved procedures. * You will be there for our donors, which includes working a variety of shifts, Saturdays and Sundays, and holidays. What you bring to Takeda: * High school diploma or equivalent * Ability to walk and/or stand for the entire work shift * Will work evenings, weekends, and holidays * Ability to lean, bend, stoop, crouch, and reach above shoulders and below knees * Ability to lift to 5 lbs., and occasional lifting of materials up to 32 lbs. and rarely 50 lbs. * Fine motor coordination, depth perception, and ability to hear equipment from a distance * Because of potential exposure to bloodborne pathogens (risk level 1), 90% of work tasks require prolonged glove wear * 1 or more years minimum experience working in a customer or patient facing role is helpful What Takeda can offer you: Every day at Takeda, we feel good knowing that what we do helps improve the lives of patients with rare diseases. At BioLife, while you focus on our donors, we will support you. We offer a purpose you can believe in, a team you can count on, opportunities for career growth, and a comprehensive benefits program to include retirement benefits, medical/dental, family leave, disability insurance and more, all in a fast-paced, friendly environment. More about us: At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to provide Better Health and a Brighter Future to people around the world. BioLife Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. For Location: USA - OH - Mentor U.S. Starting Hourly Wage: $16.00 The starting hourly wage reflects the actual starting rate for this position. The actual hourly wage offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based employees may be eligible for short-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. Locations USA - OH - Mentor Worker Type Employee Worker Sub-Type Regular Time Type Part time Job Exempt No

Hydro Pressure and Pack is growing and we want you to grow with us! We've added state-of-the-art High Pressure Processing (HPP) technology to our brand-new facility, positioning us as innovators in the food packaging industry. We're currently hiring full-time Machine Operators to join our team and help us lead the future of food safety and packaging. Our Recipe for Work/Life Balance Flexible scheduling that adapts to production needs More time at home and spend the rest of the week with your family Supportive, family-oriented workplace culture A positive work environment where your role matters Position Details Job Title: Machine Operator Job Type: Full-time Shift Options: Varying schedules based on production volume and operational needs. As a new and growing company, we offer flexibility, but shifts may change week to week. Qualifications Comfortable working in a cold environment (36-38°F) Detail-oriented with strong organizational skills Ability to prioritize tasks and work efficiently in a fast-paced environment Previous experience in food manufacturing or quality control preferred Key Responsibilities Monitor and verify production processes to ensure compliance with food safety and quality standards Accurately complete quality reports and production documentation Work with the HPP Coordinator and Production Supervisor to address quality concerns Support implementation of corrective actions and continuous improvement initiatives Ensure product meets all internal and customer specifications Perform routine inspections, including visual checks, measurements, and documentation Maintain cleanliness and sanitation in designated quality control areas Participate in training and follow all safety and hygiene protocols Perform other duties as assigned Compensation & Benefits Pay Rate: $17.00-$19.00/hour for weekday-only availability $18.00-$20.00/hour for weekend availability Comprehensive Benefits Package: Medical, dental, vision, life, accident, pet, and disability insurance 401(k) with company match Paid time off and holiday pay Free or discounted childcare services Daily company-provided lunch Additional Perks: Direct deposit or pay card options Employee referral bonuses A dedicated team committed to your success Join a team that values flexibility, quality, and work-life balance. Apply today and take the next step in a rewarding career as a Machine Operator at Hydro Pressure and Pack, where your future is fresh, fast-paced, and full of opportunity!

Valeo is a tech global company, designing breakthrough solutions to reinvent the mobility. We are an automotive supplier partner to automakers and new mobility actors worldwide. Our vision? Invent a greener and more secured mobility, thanks to solutions focusing on intuitive driving and reducing CO2 emissions. We are leader on our businesses, and recognized as one of the largest global innovative companies. Responsible for understanding and to ensure safety standards are respected, adhering to V5000, TS16949, IATF 16949, ISO 14001 and Ohio OHSAS18001 standards using QRQC methodology (All functions), Make sure, that:before starting work they understand safety working instructions at station, PPE (personal protective equipment) requirements, Conducting first level of maintenance (PM's) and first piece inspection at the start of the shift; and maintain 5S rules Responsible to understand flexibility and multiskilling requirements in their APU (Autonomous Production Unit) and to check display visual requirements are accurate. Detects problems (deviations from standards) in safety, quality and efficiency. In case a problem is detected, stops and applies the appropriate reactivity procedure. Is involved in immediate containment actions. Actively participate the improvements proposal program; Participate in 5 min meeting in APU (Autonomous Production Unit). Ensure cleanliness and safety of each workstation. Communicate any supplies shortage to the team lead at the beginning, during and after shifts. Involvement in APU continuous improvement through participation in VPS workshops Job: Production Operator Organization: Schedule: Full time Employee Status: Regular Job Type: Job Posting Date: 2024-01-24 Join Us ! Being part of our team, you will join: - one of the largest global innovative companies, with more than 20,000 engineers working in Research & Development - a multi-cultural environment that values diversity and international collaboration - more than 100,000 colleagues in 31 countries... which make a lot of opportunity for career growth - a business highly committed to limiting the environmental impact if its activities and ranked by Corporate Knights as the number one company in the automotive sector in terms of sustainable development More information on Valeo: *********************

The Special Processes Technician is responsible for finishing precision machined medical devices according to customer specifications. What You'll Do: Follow all SOP's, GMP's, GDP's Laser Etching Mastery of Visual Laser Marker software (VLM) Ultrasonic cleaning Blasting Tumbling Passivation Assemble Components Box products & apply labeling materials Follow all safety rules Follow area 5S expectations Meet all company and area expectations Other duties and responsibilities may be assigned as needed. What You'll Need: High school diploma or general education degree (GED); and one to three months related industry experience and/or training; or equivalent combination of education and experience. Ability to read, understand and follow Specification Sheets Basic mathematical skills to understand tolerances and variation Basic understanding of CNC concepts laser & parameters Experience using diagrams or blueprints and to follow other written or verbal instructions Ability to use measuring devices and hand tools Mechanically inclined with good dexterity - able to use both hand and power tools Excellent vision & hand-eye coordination Ability to work accurately in a fast-paced environment and to meet quality and quantity quotas. Able to quality check finished product ability to suggest sending unsatisfactory items to rework Proven experience with safe production standards Computer programming literacy (visual/basic script) Fluency with Microsoft Office (Access, Excel, Word) Knowledge of fixture concepts

Hours of Job The schedule is flexible, with an estimated commitment of approximately 8 hours per week. This role is well-suited for a student currently pursuing a degree in Radiography. Duties and Key Responsibilities Works under the supervision of the Radiologist, Radiologic Technologist and Radiology Transcriptionist. Operates ionizing radiation-generating equipment in the performance of standard radiography exams under the scope of the GXMO license. Assists the licensed Radiologic Technologist in performing radiological/ancillary exams. Performs clerical duties, which may include but is not limited to, patient reception, scheduling and screening. Data entry, filing answering telephones taking and delivering messages. Transports patients safely to and from Medical Imaging and other work areas. Utilizing appropriate mode of transportation for each patient and using assistive devices as necessary such as gait belt, smooth mover, hover jack and Hoyer lift. Screens MRI patients and ensures patients and other safety in the MRI environment. Respects patients' rights to privacy, dignity and confidentiality. Maintains established hospital and work area policies, procedures, objectives, quality assessment, guest relations, safety, environmental, and infection control. Communicates appropriately with interdisciplinary team and other customers. Consistently practices the behaviors of The Caring Model and Coworker Commitment. Enhances work performance by participating in in-services, staff meetings, community outreach and committees as required. Assists in inventory, care and maintenance of departmental equipment and supplies. Performs other duties as required. Requirements Ability to concentrate for long periods, work independently and exercise good judgment, keyboarding and basic computer skills. Requires full range of body motion including manual and physical dexterity, hand/eye coordination. Standing or walking minimum of 60% of the time occasionally lifts and carries up to 50 pounds. Education/Certifications High School diploma required. Currently enrolled in the final year of an accredited radiography program, recently graduated from an accredited radiology program within the past 12 months, or has completed a GXMO didactic educational program approved by the Ohio Department of Health (ODH). Licensed by the State of Ohio in the category of General X-Ray Machine Operator (GXMO) Experience Healthcare related work, previous experience in Medical Imaging preferred. Grand Lake Health System provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state and local laws. GLHS complies with applicable state and local laws governing nondiscrimination in employment in all of our locations. In addition, Grand Lake Health System is an At-Will Employment employer.